File Name: list of generic and brand name drugs .zip
Despite this variation in cost, barriers such as lack of communication and education, previous side effects, or preference may play a role in continued use of brand-name medications.
Generic Drugs. Some patients have the misperception that generic drugs are inferior to brand name drugs. Bioequivalent drug formulations have the same bioavailability; that is, the same rate and extent of absorption. New drug formulations must meet standards set by Health Canada. If the generic drug is bioequivalent, it is assumed that it will produce the same therapeutic effect as the brand name drug. This means that new clinical studies are not needed for generic drugs. This is not true.
Drug nomenclature is the systematic naming of drugs , especially pharmaceutical drugs. In the majority of circumstances, drugs have 3 types of names: chemical names , the most important of which is the IUPAC name ; generic or nonproprietary names , the most important of which are the International Nonproprietary Names INNs ; and trade names, which are brand names. Drug names are often subject to legal regulation, including approval for new drugs to avoid confusion with existing drugs and on packaging to establish clear rules about adulterants and fraudulent or misleading labeling. A national formulary  is often designated to define drug names and purity standards for regulatory purposes. The legally approved names in various countries include:.
The resources below have been provided to help narrow your search to specific, targeted drug information.
A generic drug is a pharmaceutical drug that contains the same chemical substance as a drug that was originally protected by chemical patents. Generic drugs are allowed for sale after the patents on the original drugs expire. Because the active chemical substance is the same, the medica l profile of generics is believed to be equivalent in performance. Although they may not be associated with a particular company, generic drugs are usually subject to government regulations in the countries in which they are dispensed. A generic drug must contain the same active ingredients as the original brand-name formulation.
A generic drug is a medication created to be the same as an existing approved brand-name drug in dosage form, safety, strength, route of administration, quality, and performance characteristics. A generic medicine works in the same way and provides the same clinical benefit as its brand-name version. This standard applies to all FDA-approved generic medicines. A generic medicine is the same as a brand-name medicine in dosage, safety, effectiveness, strength, stability, and quality, as well as in the way it is taken and should be used. Generic medicines use the same active ingredients as brand-name medicines and work the same way, so they have the same risks and benefits as the brand-name medicines. In addition, FDA conducts 3, inspections of manufacturing plants a year, ensuring compliance with the agency's regulations on good manufacturing practices.
Alphabetical Brand Drug/Generic Equivalent List on Website. Brand Name*. FDA-Approved Generic Drug Name. Commonly Used For**.
If you want to use a drug list to find out if we cover your medication, this information will help you understand how to read one. You can use drug lists to see if your health plan covers your prescription medication. Most of the medications on our drug lists are grouped by tiers so that you can find out if your health plan covers your prescription.
Understanding the differences between generic and brand name medications can help injured workers understand their workers' compensation prescriptions a bit better. When you experience an on-the-job accident or illness, you have to become fluent in medical jargon pretty quickly. It's helpful to know the ins and outs of the medications that your doctor prescribes.
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